Evidence map›Paper›PMID 29212015›Full record

ArticleCell reports2017

Opposing Post-transcriptional Control of InR by FMRP and LIN-28 Adjusts Stem Cell-Based Tissue Growth.

Arthur Luhur, Kasun Buddika, Ishara Surangi Ariyapala, Shengyao Chen, Nicholas Samuel Sokol

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Age-related ceRNA networks in adultFrontiers in genetics · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Dysregulation of BMP, Wnt, and Insulin Signaling in Fragile X Syndrome.Frontiers in cell and developmental biology · 2022
    Review
  11. A stress-responsive miRNA regulates BMP signaling to maintain tissue homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. I-KCKT allows dissection-free RNA profiling of adultDevelopment (Cambridge, England) · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Lar maintains the homeostasis of the hematopoietic organ inDevelopment (Cambridge, England) · 2019
    Article
  17. Article
  18. Generating and working with Drosophila cell cultures: Current challenges and opportunities.Wiley interdisciplinary reviews. Developmental biology · 2019
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Arthur LuhurDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Kasun BuddikaDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Ishara Surangi AriyapalaDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Shengyao ChenDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Nicholas Samuel SokolDepartment of Biology, Indiana University, Bloomington, IN 47405, USA. Electronic address: nsokol@indiana.edu.
Indiana University Bloomington · US

Funding

Post-transcriptional Control of Adaptive Tissue GrowthR01GM124220 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI CALVI, BRIAN R · 2017 to 2020
$1.3M
Lin-28 and the translational control of stem cell metabolismR21OD019916 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI SOKOL, NICHOLAS · 2015 to 2016
$409k
NIGMS NIH HHS R01 GM124220NIH HHS R21 OD019916
6 · The paper itself

Abstract

Although the intrinsic mechanisms that control whether stem cells divide symmetrically or asymmetrically underlie tissue growth and homeostasis, they remain poorly defined. We report that the RNA-binding protein fragile X mental retardation protein (FMRP) limits the symmetric division, and resulting expansion, of the stem cell population during adaptive intestinal growth in Drosophila. The elevated insulin sensitivity that FMRP-deficient progenitor cells display contributes to their accelerated expansion, which is suppressed by the depletion of insulin-signaling components. This FMRP activity is mediated solely via a second conserved RNA-binding protein, LIN-28, known to boost insulin signaling in stem cells. Via LIN-28, FMRP controls progenitor cell behavior by post-transcriptionally repressing the level of insulin receptor (InR). This study identifies the stem cell-based mechanism by which FMRP controls tissue adaptation, and it raises the possibility that defective adaptive growth underlies the accelerated growth, gastrointestinal, and other symptoms that affect fragile X syndrome patients.

Indexed as

AnimalsDrosophila ProteinsFemaleFragile X Messenger Ribonucleoprotein 1IntestinesReceptor Protein-Tyrosine KinasesRNA-Binding ProteinsStem CellsDrosophila ProteinsFragile X Messenger Ribonucleoprotein 1InR protein, DrosophilaLin-28 protein, DrosophilaReceptor Protein-Tyrosine KinasesRNA-Binding Proteinsadaptive growthfmr1FMRPIISinsulin receptorinsulin sensitivityintestinal stem cellLIN-28tissue resizing

Identifiers

PMID29212015
PMCPMC5728658
OpenAlexW2772570926

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.